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MATRIX platform to analyze translation machinery remodeling in glioblastoma cells

Here, we present a protocol using MATRIX (mass spectrometry analysis of active translation factors using ribosome density fractionation and isotopic labeling experiments) platform to investigate changes of the protein synthesis machinery in U87MG glioblastoma cells in response to the rocaglate silve...

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Detalles Bibliográficos
Autores principales: Ho, J.J. David, Cunningham, Tyler A., Krieger, Jonathan R., Schatz, Jonathan H., Lee, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763746/
https://www.ncbi.nlm.nih.gov/pubmed/36595908
http://dx.doi.org/10.1016/j.xpro.2022.101919
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author Ho, J.J. David
Cunningham, Tyler A.
Krieger, Jonathan R.
Schatz, Jonathan H.
Lee, Stephen
author_facet Ho, J.J. David
Cunningham, Tyler A.
Krieger, Jonathan R.
Schatz, Jonathan H.
Lee, Stephen
author_sort Ho, J.J. David
collection PubMed
description Here, we present a protocol using MATRIX (mass spectrometry analysis of active translation factors using ribosome density fractionation and isotopic labeling experiments) platform to investigate changes of the protein synthesis machinery in U87MG glioblastoma cells in response to the rocaglate silvestrol. This protocol describes steps to perform SILAC (stable isotope labeling by amino acids in cell culture), ribosome density fractionation, protein isolation, and mass spectrometry analysis. This approach can be applied to study any adaptive remodeling of protein synthesis machineries. For complete details on the use and execution of this protocol, please refer to Ho et al. (2021).(1)
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spelling pubmed-97637462022-12-21 MATRIX platform to analyze translation machinery remodeling in glioblastoma cells Ho, J.J. David Cunningham, Tyler A. Krieger, Jonathan R. Schatz, Jonathan H. Lee, Stephen STAR Protoc Protocol Here, we present a protocol using MATRIX (mass spectrometry analysis of active translation factors using ribosome density fractionation and isotopic labeling experiments) platform to investigate changes of the protein synthesis machinery in U87MG glioblastoma cells in response to the rocaglate silvestrol. This protocol describes steps to perform SILAC (stable isotope labeling by amino acids in cell culture), ribosome density fractionation, protein isolation, and mass spectrometry analysis. This approach can be applied to study any adaptive remodeling of protein synthesis machineries. For complete details on the use and execution of this protocol, please refer to Ho et al. (2021).(1) Elsevier 2022-12-09 /pmc/articles/PMC9763746/ /pubmed/36595908 http://dx.doi.org/10.1016/j.xpro.2022.101919 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Ho, J.J. David
Cunningham, Tyler A.
Krieger, Jonathan R.
Schatz, Jonathan H.
Lee, Stephen
MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title_full MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title_fullStr MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title_full_unstemmed MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title_short MATRIX platform to analyze translation machinery remodeling in glioblastoma cells
title_sort matrix platform to analyze translation machinery remodeling in glioblastoma cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763746/
https://www.ncbi.nlm.nih.gov/pubmed/36595908
http://dx.doi.org/10.1016/j.xpro.2022.101919
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